Cytokinesis in Aspergillus nidulans is controlled by cell size, nuclear positioning and mitosis

J Cell Sci. 1996 Aug:109 ( Pt 8):2179-88. doi: 10.1242/jcs.109.8.2179.

Abstract

The mycelium of Aspergillus nidulans is composed of multinucleate cellular compartments delimited by crosswalls called septa. Septum formation is dependent on mitosis and requires the recruitment of actin to the site of septum formation. Employing a collection of temperature sensitive nuclear distribution (nudA2, nudC3 and nudF7), nuclear division (nimA5, hfaB3), and septation (sepD5, sepG1) mutants, we have investigated the interdependency among nuclear positioning, mitosis, and cell growth in structuring the cellular compartments of A. nidulans. The cellular compartments of nud+ strains were highly uniform with regard to nuclear distribution and averaged 38 microns in length. Incubation of nud mutants at semi-restrictive temperature resulted in aberrant nuclear distribution that appeared to direct the formation of variable-sized cellular compartments, ranging from 5 microns to greater than 81 microns. In germinating spores, the first septum forms at the basal end of the germ tube following the third round of nuclear division. Germlings must undergo mitosis in order to form a septum. Temperature-sensitive mitotic mutants were used to show that a single nuclear division is sufficient to activate septum formation, provided a critical cell size has been attained. In mitotic mutants and wild-type cells, delays in nuclear division resulted in the misplacement of the first septum. These results strongly support the role of mitotic nuclei in determining septal placement, and suggest that cell size control is post-mitotic in A. nidulans.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aspergillus nidulans / cytology*
  • Aspergillus nidulans / genetics
  • Cell Compartmentation
  • Cell Cycle Proteins*
  • Cell Division*
  • Cell Nucleus / ultrastructure*
  • Dyneins / metabolism
  • Fungal Proteins / metabolism
  • Mitosis*
  • NIMA-Related Kinase 1
  • NIMA-Related Kinases
  • Nuclear Proteins / metabolism
  • Protein Serine-Threonine Kinases / metabolism

Substances

  • Cell Cycle Proteins
  • Fungal Proteins
  • NUDC protein, Emericella nidulans
  • NUDF protein, Emericella nidulans
  • Nuclear Proteins
  • apsA protein, Aspergillus nidulans
  • NIMA-Related Kinase 1
  • NIMA-Related Kinases
  • NIMA-related kinase 6
  • Protein Serine-Threonine Kinases
  • Dyneins
  • NUDA protein, Emericella nidulans